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Mixed-metal hybrid ultramicroporous material (HUM) precursor to graphene-supported tetrataenite as a highly active and durable NPG catalyst for the OER.

Authors :
Haikal, Rana R.
Kumar, Amrit
O'Nolan, Daniel
Kumar, Naveen
Karakalos, Stavros G.
Hassanien, Abdou
Zaworotko, Michael J.
Alkordi, Mohamed H.
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry; 4/21/2021, Vol. 50 Issue 15, p5311-5317, 7p
Publication Year :
2021

Abstract

Current interest in investigating non-precious group (NPG) metals for catalyzing the oxygen evolution reaction (OER) has revealed that doping of Ni hydroxides with Fe results in the dramatic enhancement of catalytic activity. Herein, a facile pathway to construct tetrataenite, an NiFe alloy of extraterrestrial origin and to address the limited electrical conductivity of metal oxides/hydroxides by directly constructing them atop graphene sheets is described. In this approach, a one-pot, bottom-up assembly of hybrid ultramicroporous materials (HUMs) was carried out, in the presence of suspended graphene (G), to homogeneously deposit the HUMs on unmodified graphene sheets, affording HUMs@G. Single metal (SIFSIX-3-Ni@G) and mixed metal (SIFSIX-3-NiFe@G) HUMs can be readily synthesized from their respective metal salts to afford a well-designed catalyst for the OER. The pyrolysis of SIFSIX-3-NiFe@G resulted in the deposition of the nanoalloy tetrataenite on G, demonstrating an exceptionally low OER onset potential of 1.44 V vs. RHE and reduced overpotential at 10 mA cm<superscript>−2</superscript> (η<subscript>10</subscript> = 266 mV). The synergy between the composition of the active catalyst and the electronically conductive support was attained by designing a reaction system encoding the self-assembly of a crystalline pre-catalyst on G sheets. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
50
Issue :
15
Database :
Complementary Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
149918681
Full Text :
https://doi.org/10.1039/d0dt04118a